Rappold GA - Search Results

1

Investigation of SHANK3 in schizophrenia.

de Sena Cortabitarte A, Degenhardt F, Strohmaier J, Lang M, Weiss B, Roeth R, Giegling I, Heilmann-Heimbach S, Hofmann A, Rujescu D, Fischer C, Rietschel M, Nöthen MM, Rappold GA, Berkel S. de Sena Cortabitarte A, et al. Among authors: rappold ga. Am J Med Genet B Neuropsychiatr Genet. 2017 Jun;174(4):390-398. doi: 10.1002/ajmg.b.32528. Epub 2017 Mar 28. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 28371232

2

Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients.

Frank B, Niesler B, Nöthen MM, Neidt H, Propping P, Bondy B, Rietschel M, Maier W, Albus M, Rappold G. Frank B, et al. Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):1-5. doi: 10.1002/ajmg.b.30070. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15389765

3

Identification and functional characterization of rare SHANK2 variants in schizophrenia.

Peykov S, Berkel S, Schoen M, Weiss K, Degenhardt F, Strohmaier J, Weiss B, Proepper C, Schratt G, Nöthen MM, Boeckers TM, Rietschel M, Rappold GA. Peykov S, et al. Among authors: rappold ga. Mol Psychiatry. 2015 Dec;20(12):1489-98. doi: 10.1038/mp.2014.172. Epub 2015 Jan 6. Mol Psychiatry. 2015. PMID: 25560758 Free PMC article.

4

Rare SHANK2 variants in schizophrenia.

Peykov S, Berkel S, Degenhardt F, Rietschel M, Nöthen MM, Rappold GA. Peykov S, et al. Among authors: rappold ga. Mol Psychiatry. 2015 Dec;20(12):1487-8. doi: 10.1038/mp.2015.122. Epub 2015 Aug 25. Mol Psychiatry. 2015. PMID: 26303658 Free PMC article. No abstract available.

5

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation.

Berkel S, Marshall CR, Weiss B, Howe J, Roeth R, Moog U, Endris V, Roberts W, Szatmari P, Pinto D, Bonin M, Riess A, Engels H, Sprengel R, Scherer SW, Rappold GA. Berkel S, et al. Among authors: rappold ga. Nat Genet. 2010 Jun;42(6):489-91. doi: 10.1038/ng.589. Epub 2010 May 16. Nat Genet. 2010. PMID: 20473310

6

Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family.

Rafiullah R, Aslamkhan M, Paramasivam N, Thiel C, Mustafa G, Wiemann S, Schlesner M, Wade RC, Rappold GA, Berkel S. Rafiullah R, et al. Among authors: rappold ga. J Med Genet. 2016 Feb;53(2):138-44. doi: 10.1136/jmedgenet-2015-103179. Epub 2015 Nov 13. J Med Genet. 2016. PMID: 26566883

7

A direct regulatory link between microRNA-137 and SHANK2: implications for neuropsychiatric disorders.

de Sena Cortabitarte A, Berkel S, Cristian FB, Fischer C, Rappold GA. de Sena Cortabitarte A, et al. Among authors: rappold ga. J Neurodev Disord. 2018 Apr 17;10(1):15. doi: 10.1186/s11689-018-9233-1. J Neurodev Disord. 2018. PMID: 29665782 Free PMC article.

8

Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patients.

Niesler B, Weiss B, Fischer C, Nöthen MM, Propping P, Bondy B, Rietschel M, Maier W, Albus M, Franzek E, Rappold GA. Niesler B, et al. Among authors: rappold ga. Pharmacogenetics. 2001 Feb;11(1):21-7. doi: 10.1097/00008571-200102000-00003. Pharmacogenetics. 2001. PMID: 11207027

9

A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders.

Hammer C, Degenhardt F, Priebe L, Stütz AM, Heilmann S, Waszak SM, Schlattl A, Mangold E, Hoffmann P, Nöthen MM, Rietschel M, Rappold G, Korbel J, Cichon S, Niesler B; MooDS Consortium. Hammer C, et al. Bipolar Disord. 2014 Nov;16(7):764-8. doi: 10.1111/bdi.12207. Epub 2014 Apr 23. Bipolar Disord. 2014. PMID: 24754353

10

Inherited and de novo SHANK2 variants associated with autism spectrum disorder impair neuronal morphogenesis and physiology.

Berkel S, Tang W, Treviño M, Vogt M, Obenhaus HA, Gass P, Scherer SW, Sprengel R, Schratt G, Rappold GA. Berkel S, et al. Among authors: rappold ga. Hum Mol Genet. 2012 Jan 15;21(2):344-57. doi: 10.1093/hmg/ddr470. Epub 2011 Oct 12. Hum Mol Genet. 2012. PMID: 21994763 Free PMC article.

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